A de novo complex chromosome rearrangement involving chromosomes 2, 3, 5, 9 and 11 detected prenatally and studied postnatally by conventional cytogenetics and molecular cytogenetic analyses

Fetal Diagnosis and Therapy

Volumn 22, Issue 4, 2007, Pages 249-253

  Mechoso, Búrix ^a   Vaglio, Alicia ^a   Quadrelli, Andrea ^a   Mark, Hon Fong L ^b   Huang, Xin Li ^b   Milunsky, Aubrey ^b   Quadrelli, Roberto ^a  

^a Hospital Italiano Montevideo   (Uruguay)

^b BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Comparative genomic hybridization; Complex chromosome rearrangements; Fluorescence in situ hybridization; Genetic counseling; Prenatal postnatal diagnosis

Indexed keywords

ADULT; ARTICLE; C BANDING; CASE REPORT; CHROMOSOME 11; CHROMOSOME 2; CHROMOSOME 3; CHROMOSOME 5; CHROMOSOME 9; CHROMOSOME ANALYSIS; CHROMOSOME INSERTION; CHROMOSOME INVERSION; CHROMOSOME REARRANGEMENT; CHROMOSOME TRANSLOCATION; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL MALFORMATION; FEMALE; FETUS KARYOTYPING; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPE 46,XY; MOLECULAR GENETICS; NEWBORN; PERINATAL PERIOD; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; PSYCHOMOTOR DEVELOPMENT;

ADULT; CHROMOSOME ABERRATIONS; CHROMOSOME BANDING; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 2; CHROMOSOMES, HUMAN, PAIR 3; CHROMOSOMES, HUMAN, PAIR 5; CHROMOSOMES, HUMAN, PAIR 9; CYTOGENETIC ANALYSIS; FEMALE; GENETIC COUNSELING; GENETIC SCREENING; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; LIVE BIRTH; NUCLEIC ACID HYBRIDIZATION; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 34250342655     PISSN: 10153837     EISSN: None     Source Type: Journal    
DOI: 10.1159/000100784     Document Type: Article

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